RecruitingNot ApplicableNCT07494812

Examining the Feasibility of Using Pressure Gradient Regulated Automated Cerebral Spinal Fluid Drainage During External Lumbar Drain Trials


Sponsor

University of Texas Southwestern Medical Center

Enrollment

10 participants

Start Date

May 14, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The intellidrop device is an FDA-approved system that automates safe, small volume of cerebral spinal fluid drainage with continuous pressure monitoring, reducing nursing workload and human error while improving patient mobility and comfort


Eligibility

Min Age: 60 YearsMax Age: 99 Years

Inclusion Criteria1

  • All patients will be adults aged 60 years or older with suspected iNPH who are being admitted to the hospital for the purpose of an LDT specifically to evaluate for benefit from shunt placement.

Exclusion Criteria1

  • Patients who are under 18 years of age, pregnant, or are currently incarcerated will be excluded from participating in this study.

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Interventions

DEVICEIntellidrop Automated CSF Drainage System

Participants will undergo lumbar drainage using the Intellidrop automated cerebrospinal fluid drainage system that monitors intracranial or spinal pressure and manages external drainage of cerebrospinal fluid and other body fluids to a user selected pressure target or volume target. Its closed loop, gravity-based drainage ensures natural flow, while offering position-agnostic precision control to achieve an hourly target volume. It connects to the distal end of the lumbar catheter outside the body and replaces the drainage collection device and manual nursing effort.

DEVICEIntellidrop Automated CSF Drainage System

Participants will undergo lumbar drainage using the Intellidrop automated cerebrospinal fluid drainage system that provides continuous intracranial pressure monitoring and automated control of CSF removal. It is programmed to withdraw small frequent volumes of CSF within predefined safety limits reducing the need for manual stopcock adjustments and minimizing human error. It is designed to improve workflow efficiency, enhance patient mobility, and evaluate the device;s feasibility, performance and safety during the lumbar drain.


Locations(1)

UT Southwestern Medical Center

Dallas, Texas, United States

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NCT07494812